Data Entry In Rims / Regulatory Affairs

buscojobs España; Zaragoza; A distancia; EUR 30.000 - 45.000; Jornada completa

Descripción de la vacante

A leading company in the pharmaceutical sector is seeking a Data Management professional to join their Barcelona team. This role involves data entry in Veeva Vault, regulatory support, and maintaining data accuracy. The position offers a hybrid or remote work model, providing flexibility for candidates across Spain. Ideal candidates will have a relevant degree and experience in the pharmaceutical industry, along with strong communication and attention to detail.

Servicios

Homeoffice & Hybrid or Remote Model

Training and personal development programs

Formación

• Bachelor’s or equivalent in relevant fields.
• Experience in the pharmaceutical sector is an asset.
• Familiarity with Veeva Vault and data management standards is highly valued.

Responsabilidades

• Accurate data entry and management in Veeva Vault.
• Support regulatory operations and maintain data quality.
• Engage with team and clients for data management tasks.

Conocimientos

Data Entry

Regulatory Knowledge

Communication Skills

Attention to Detail

Educación

Bachelor’s in Pharma / Science / IT or Data Management

Herramientas

Veeva Vault

Descripción del empleo

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Client : ASPHALION

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EU work permit required :

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Job Reference :

741714398886127206432460

Job Views : Posted :

31.03.2025

Expiry Date : 15.05.2025

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Job Description :

Join our Barcelona team and work with the Data Management unit. Leverage your skills in Veeva Vault and data entry to support our projects.

Tasks & Responsibilities :

Data Entry in Veeva Vault, such as :

• Accurately input and manage data related to new applications, including MAA / NDA / BLA / JND
• Regulatory Operations Support (such as WorkSharing, withdrawals, licensing…)
• International Data Management (Apollo, APAC master files)
• Complex Data Entry Tasks (bundling / splitting activities, Activity / RO / Submission Status updates, RAT updates, and creating objects)

Key Activities :

1. Continuous Data Input and Accuracy.
2. Data Quality checks.
3. Regulatory Document Management.
4. Maintenance of data.
5. Contacts with team and clients.

Requirements :

• Bachelor’s or FP or other studies in Pharma / Science / IT or Data Management related fields.
• Previous experience in the pharmaceutical sector is an asset.
• Familiarity with Veeva Vault or other RIMS, Data Entry, Regulatory knowledge, and xEVMPD / IDMP standards is highly valued.
• Proactive, good communication skills, accurate, and detail-oriented.

Why work at Asphalion?

Homeoffice & Hybrid or Remote Model (You can be located anywhere in Spain!)

Wide variety of projects, new challenges, and experiences.

Training and personal development programs.

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